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Opening the lid on piano-stool complexes: An account of ruthenium(II)–arene complexes with medicinal applications

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TLDR
The origins of the field are described, the design of compounds that inhibit enzymes are designed, the application of multinuclear systems to act as drug delivery vehicles, and the development of bioanalytical and biophysical methods are highlighted to help elucidate the mechanisms by which these compounds function.
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This article is published in Journal of Organometallic Chemistry.The article was published on 2014-02-01. It has received 226 citations till now.

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Citations
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Antitumour metal compounds: more than theme and variations

TL;DR: The recent achievement of oxaliplatin for the treatment of colon cancer should not belie the imbalance between a plethora of investigated complexes and a very small number of clinically approved platinum drugs.
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Ferrocifen type anti cancer drugs.

TL;DR: It is shown here the different antitumoral approaches offered by ferrocifen derivatives, originally simple derivatives of tamoxifen, which over the course of their development have proved to possess remarkable structural and mechanistic diversity.
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The development of RAPTA compounds for the treatment of tumors

TL;DR: Ruthenium(II)-arene RAPTA-type compounds have been extensively explored for their medicinal properties and a comprehensive review of this class of compounds is provided in this article.
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Metal-based drugs that break the rules

TL;DR: This work highlights compounds that are apparently incompatible with the more classical (platinum-derived) concepts employed in the development of metal-based anticancer drugs, with respect to both compound design and the approaches used to validate their utility.
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Recent advances in supramolecular and biological aspects of arene ruthenium(II) complexes

TL;DR: A review of the recent developments of arene ruthenium complexes towards both supramolecular chemistry and biology can be found in this paper, where the authors focus on the recent development of these compounds towards both biology and chemistry.
References
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Journal ArticleDOI

In silico evolution of substrate selectivity: comparison of organometallic ruthenium complexes with the anticancer drug cisplatin.

TL;DR: A comparative quantum chemical approach helps to clarify how the selectivity of anticancer metallopharmaceuticals towards potential biological targets can be controlled by metal and ligands.
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Rationalization of the inhibition activity of structurally related organometallic compounds against the drug target cathepsin B by DFT

TL;DR: Initial structure-activity relationships have been defined with the calculated binding energies of the M-S bonds correlating well with the observed inhibition properties of the compounds, which showed similar enzyme inhibition properties to NAMI-A.
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DNA interactions of dinuclear RuII arene antitumor complexes in cell-free media

TL;DR: The concept for the design of interhelical and DNA-protein cross-linking agents based on dinuclear Ru(II) arene complexes with sufficiently long linkers between two Ru centers may result in new compounds which exhibit a variety of biological effects and can be also useful in nucleic acids research.
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Influence of Structural Variation on the Anticancer Activity of RAPTA-Type Complexes: ptn versus pta

TL;DR: In this paper, the reactivity of the RAPTA complexes toward double-stranded oligonucleotides and the model protein ubiquitin was studied using Fourier transform ICR mass spectrometry (FT-ICR-MS) and gel electrophoresis.
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Anticancer Activity of Self-Assembled Molecular Rectangles via Arene-Ruthenium Acceptors and a New Unsymmetrical Amide Ligand.

TL;DR: The cytotoxicity of rectangle 5 was found to be considerably stronger against all cancer cell lines than that of the reference drug cisplatin, and the cytotoxicities of both rectangles have been established against Colo320 (colorectal cancer), A549 (lung cancer), MCF-7 (breast cancer) and H1299 ( lung cancer) human cancer cell Lines.
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